Apollo lens corrective spectacle lens (Non-sterile)
- Analysis ID
- 8ffc3cc411119acd7a10f283d239dc8a
- License Form
- Ministry of Health Medical Device Import No. 013388
- Customs Code
- DHA09401338807
- Manufacturer
- FUJITA OPTICAL CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- HKO OPTICAL LENS (TAIWAN) CO., LTD.
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Corrective Lenses (M.5844)".
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M5844 corrective lenses
- Import Information
- Imported from abroad
- Registration Date
- Sep 05, 2013
- Expiry Date
- Sep 05, 2023
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Access comprehensive regulatory information for Apollo lens corrective spectacle lens (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8ffc3cc411119acd7a10f283d239dc8a and manufactured by FUJITA OPTICAL CO., LTD.. The authorized representative in Taiwan is HKO OPTICAL LENS (TAIWAN) CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HONG KONG OPTICAL LENS CO., LTD., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.